Development of a Highly Effective African Swine Fever Virus Vaccine by Deletion of the I177L Gene Results in Sterile Immunity against the Current Epidemic Eurasia Strain
Currently, there is no commercially available vaccine against African swine fever. Outbreaks of this disease are devastating the swine industry from Central Europe to East Asia, and they are being caused by circulating strains of African swine fever virus derived from the Georgia 2007 isolate. Here,...
Saved in:
Published in | Journal of virology Vol. 94; no. 7 |
---|---|
Main Authors | , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
American Society for Microbiology
17.03.2020
|
Subjects | |
Online Access | Get full text |
Cover
Loading…
Abstract | Currently, there is no commercially available vaccine against African swine fever. Outbreaks of this disease are devastating the swine industry from Central Europe to East Asia, and they are being caused by circulating strains of African swine fever virus derived from the Georgia 2007 isolate. Here, we report the discovery of a previously uncharacterized virus gene, which when deleted completely attenuates the Georgia isolate. Importantly, animals infected with this genetically modified virus were protected from developing ASF after challenge with the virulent parental virus. Interestingly, ASFV-G-ΔI177L confers protection even at low doses (10
2
HAD
50
) and remains completely attenuated when inoculated at high doses (10
6
HAD
50
), demonstrating its potential as a safe vaccine candidate. At medium or higher doses (10
4
HAD
50
), sterile immunity is achieved. Therefore, ASFV-G-ΔI177L is a novel efficacious experimental ASF vaccine protecting pigs from the epidemiologically relevant ASFV Georgia isolate.
African swine fever virus (ASFV) is the etiological agent of a contagious and often lethal disease of domestic pigs that has significant economic consequences for the swine industry. The disease is devastating the swine industry in Central Europe and East Asia, with current outbreaks caused by circulating strains of ASFV derived from the 2007 Georgia isolate (ASFV-G), a genotype II ASFV. In the absence of any available vaccines, African swine fever (ASF) outbreak containment relies on the control and culling of infected animals. Limited cross-protection studies suggest that in order to ensure a vaccine is effective, it must be derived from the current outbreak strain or at the very least from an isolate with the same genotype. Here, we report the discovery that the deletion of a previously uncharacterized gene, I177L, from the highly virulent ASFV-G produces complete virus attenuation in swine. Animals inoculated intramuscularly with the virus lacking the I177L gene, ASFV-G-ΔI177L, at a dose range of 10
2
to 10
6
50% hemadsorbing doses (HAD
50
), remained clinically normal during the 28-day observational period. All ASFV-G-ΔI177L-infected animals had low viremia titers, showed no virus shedding, and developed a strong virus-specific antibody response; importantly, they were protected when challenged with the virulent parental strain ASFV-G. ASFV-G-ΔI177L is one of the few experimental vaccine candidate virus strains reported to be able to induce protection against the ASFV Georgia isolate, and it is the first vaccine capable of inducing sterile immunity against the current ASFV strain responsible for recent outbreaks.
IMPORTANCE
Currently, there is no commercially available vaccine against African swine fever. Outbreaks of this disease are devastating the swine industry from Central Europe to East Asia, and they are being caused by circulating strains of African swine fever virus derived from the Georgia 2007 isolate. Here, we report the discovery of a previously uncharacterized virus gene, which when deleted completely attenuates the Georgia isolate. Importantly, animals infected with this genetically modified virus were protected from developing ASF after challenge with the virulent parental virus. Interestingly, ASFV-G-ΔI177L confers protection even at low doses (10
2
HAD
50
) and remains completely attenuated when inoculated at high doses (10
6
HAD
50
), demonstrating its potential as a safe vaccine candidate. At medium or higher doses (10
4
HAD
50
), sterile immunity is achieved. Therefore, ASFV-G-ΔI177L is a novel efficacious experimental ASF vaccine protecting pigs from the epidemiologically relevant ASFV Georgia isolate. |
---|---|
AbstractList | Currently, there is no commercially available vaccine against African swine fever. Outbreaks of this disease are devastating the swine industry from Central Europe to East Asia, and they are being caused by circulating strains of African swine fever virus derived from the Georgia 2007 isolate. Here, we report the discovery of a previously uncharacterized virus gene, which when deleted completely attenuates the Georgia isolate. Importantly, animals infected with this genetically modified virus were protected from developing ASF after challenge with the virulent parental virus. Interestingly, ASFV-G-ΔI177L confers protection even at low doses (10
2
HAD
50
) and remains completely attenuated when inoculated at high doses (10
6
HAD
50
), demonstrating its potential as a safe vaccine candidate. At medium or higher doses (10
4
HAD
50
), sterile immunity is achieved. Therefore, ASFV-G-ΔI177L is a novel efficacious experimental ASF vaccine protecting pigs from the epidemiologically relevant ASFV Georgia isolate.
African swine fever virus (ASFV) is the etiological agent of a contagious and often lethal disease of domestic pigs that has significant economic consequences for the swine industry. The disease is devastating the swine industry in Central Europe and East Asia, with current outbreaks caused by circulating strains of ASFV derived from the 2007 Georgia isolate (ASFV-G), a genotype II ASFV. In the absence of any available vaccines, African swine fever (ASF) outbreak containment relies on the control and culling of infected animals. Limited cross-protection studies suggest that in order to ensure a vaccine is effective, it must be derived from the current outbreak strain or at the very least from an isolate with the same genotype. Here, we report the discovery that the deletion of a previously uncharacterized gene, I177L, from the highly virulent ASFV-G produces complete virus attenuation in swine. Animals inoculated intramuscularly with the virus lacking the I177L gene, ASFV-G-ΔI177L, at a dose range of 10
2
to 10
6
50% hemadsorbing doses (HAD
50
), remained clinically normal during the 28-day observational period. All ASFV-G-ΔI177L-infected animals had low viremia titers, showed no virus shedding, and developed a strong virus-specific antibody response; importantly, they were protected when challenged with the virulent parental strain ASFV-G. ASFV-G-ΔI177L is one of the few experimental vaccine candidate virus strains reported to be able to induce protection against the ASFV Georgia isolate, and it is the first vaccine capable of inducing sterile immunity against the current ASFV strain responsible for recent outbreaks.
IMPORTANCE
Currently, there is no commercially available vaccine against African swine fever. Outbreaks of this disease are devastating the swine industry from Central Europe to East Asia, and they are being caused by circulating strains of African swine fever virus derived from the Georgia 2007 isolate. Here, we report the discovery of a previously uncharacterized virus gene, which when deleted completely attenuates the Georgia isolate. Importantly, animals infected with this genetically modified virus were protected from developing ASF after challenge with the virulent parental virus. Interestingly, ASFV-G-ΔI177L confers protection even at low doses (10
2
HAD
50
) and remains completely attenuated when inoculated at high doses (10
6
HAD
50
), demonstrating its potential as a safe vaccine candidate. At medium or higher doses (10
4
HAD
50
), sterile immunity is achieved. Therefore, ASFV-G-ΔI177L is a novel efficacious experimental ASF vaccine protecting pigs from the epidemiologically relevant ASFV Georgia isolate. African swine fever virus (ASFV) is the etiological agent of a contagious and often lethal disease of domestic pigs that has significant economic consequences for the swine industry. The disease is devastating the swine industry in Central Europe and East Asia, with current outbreaks caused by circulating strains of ASFV derived from the 2007 Georgia isolate (ASFV-G), a genotype II ASFV. In the absence of any available vaccines, African swine fever (ASF) outbreak containment relies on the control and culling of infected animals. Limited cross-protection studies suggest that in order to ensure a vaccine is effective, it must be derived from the current outbreak strain or at the very least from an isolate with the same genotype. Here, we report the discovery that the deletion of a previously uncharacterized gene, I177L, from the highly virulent ASFV-G produces complete virus attenuation in swine. Animals inoculated intramuscularly with the virus lacking the I177L gene, ASFV-G-ΔI177L, at a dose range of 10 to 10 50% hemadsorbing doses (HAD ), remained clinically normal during the 28-day observational period. All ASFV-G-ΔI177L-infected animals had low viremia titers, showed no virus shedding, and developed a strong virus-specific antibody response; importantly, they were protected when challenged with the virulent parental strain ASFV-G. ASFV-G-ΔI177L is one of the few experimental vaccine candidate virus strains reported to be able to induce protection against the ASFV Georgia isolate, and it is the first vaccine capable of inducing sterile immunity against the current ASFV strain responsible for recent outbreaks. Currently, there is no commercially available vaccine against African swine fever. Outbreaks of this disease are devastating the swine industry from Central Europe to East Asia, and they are being caused by circulating strains of African swine fever virus derived from the Georgia 2007 isolate. Here, we report the discovery of a previously uncharacterized virus gene, which when deleted completely attenuates the Georgia isolate. Importantly, animals infected with this genetically modified virus were protected from developing ASF after challenge with the virulent parental virus. Interestingly, ASFV-G-ΔI177L confers protection even at low doses (10 HAD ) and remains completely attenuated when inoculated at high doses (10 HAD ), demonstrating its potential as a safe vaccine candidate. At medium or higher doses (10 HAD ), sterile immunity is achieved. Therefore, ASFV-G-ΔI177L is a novel efficacious experimental ASF vaccine protecting pigs from the epidemiologically relevant ASFV Georgia isolate. African swine fever virus (ASFV) is the etiological agent of a contagious and often lethal disease of domestic pigs that has significant economic consequences for the swine industry. The disease is devastating the swine industry in Central Europe and East Asia, with current outbreaks caused by circulating strains of ASFV derived from the 2007 Georgia isolate (ASFV-G), a genotype II ASFV. In the absence of any available vaccines, African swine fever (ASF) outbreak containment relies on the control and culling of infected animals. Limited cross-protection studies suggest that in order to ensure a vaccine is effective, it must be derived from the current outbreak strain or at the very least from an isolate with the same genotype. Here, we report the discovery that the deletion of a previously uncharacterized gene, I177L, from the highly virulent ASFV-G produces complete virus attenuation in swine. Animals inoculated intramuscularly with the virus lacking the I177L gene, ASFV-G-ΔI177L, at a dose range of 102 to 106 50% hemadsorbing doses (HAD50), remained clinically normal during the 28-day observational period. All ASFV-G-ΔI177L-infected animals had low viremia titers, showed no virus shedding, and developed a strong virus-specific antibody response; importantly, they were protected when challenged with the virulent parental strain ASFV-G. ASFV-G-ΔI177L is one of the few experimental vaccine candidate virus strains reported to be able to induce protection against the ASFV Georgia isolate, and it is the first vaccine capable of inducing sterile immunity against the current ASFV strain responsible for recent outbreaks.IMPORTANCE Currently, there is no commercially available vaccine against African swine fever. Outbreaks of this disease are devastating the swine industry from Central Europe to East Asia, and they are being caused by circulating strains of African swine fever virus derived from the Georgia 2007 isolate. Here, we report the discovery of a previously uncharacterized virus gene, which when deleted completely attenuates the Georgia isolate. Importantly, animals infected with this genetically modified virus were protected from developing ASF after challenge with the virulent parental virus. Interestingly, ASFV-G-ΔI177L confers protection even at low doses (102 HAD50) and remains completely attenuated when inoculated at high doses (106 HAD50), demonstrating its potential as a safe vaccine candidate. At medium or higher doses (104 HAD50), sterile immunity is achieved. Therefore, ASFV-G-ΔI177L is a novel efficacious experimental ASF vaccine protecting pigs from the epidemiologically relevant ASFV Georgia isolate.African swine fever virus (ASFV) is the etiological agent of a contagious and often lethal disease of domestic pigs that has significant economic consequences for the swine industry. The disease is devastating the swine industry in Central Europe and East Asia, with current outbreaks caused by circulating strains of ASFV derived from the 2007 Georgia isolate (ASFV-G), a genotype II ASFV. In the absence of any available vaccines, African swine fever (ASF) outbreak containment relies on the control and culling of infected animals. Limited cross-protection studies suggest that in order to ensure a vaccine is effective, it must be derived from the current outbreak strain or at the very least from an isolate with the same genotype. Here, we report the discovery that the deletion of a previously uncharacterized gene, I177L, from the highly virulent ASFV-G produces complete virus attenuation in swine. Animals inoculated intramuscularly with the virus lacking the I177L gene, ASFV-G-ΔI177L, at a dose range of 102 to 106 50% hemadsorbing doses (HAD50), remained clinically normal during the 28-day observational period. All ASFV-G-ΔI177L-infected animals had low viremia titers, showed no virus shedding, and developed a strong virus-specific antibody response; importantly, they were protected when challenged with the virulent parental strain ASFV-G. ASFV-G-ΔI177L is one of the few experimental vaccine candidate virus strains reported to be able to induce protection against the ASFV Georgia isolate, and it is the first vaccine capable of inducing sterile immunity against the current ASFV strain responsible for recent outbreaks.IMPORTANCE Currently, there is no commercially available vaccine against African swine fever. Outbreaks of this disease are devastating the swine industry from Central Europe to East Asia, and they are being caused by circulating strains of African swine fever virus derived from the Georgia 2007 isolate. Here, we report the discovery of a previously uncharacterized virus gene, which when deleted completely attenuates the Georgia isolate. Importantly, animals infected with this genetically modified virus were protected from developing ASF after challenge with the virulent parental virus. Interestingly, ASFV-G-ΔI177L confers protection even at low doses (102 HAD50) and remains completely attenuated when inoculated at high doses (106 HAD50), demonstrating its potential as a safe vaccine candidate. At medium or higher doses (104 HAD50), sterile immunity is achieved. Therefore, ASFV-G-ΔI177L is a novel efficacious experimental ASF vaccine protecting pigs from the epidemiologically relevant ASFV Georgia isolate. |
Author | Gladue, Douglas P. Holinka, Lauren G. Silva, Ediane Borca, Manuel V. Rai, Ayushi Pruitt, Sarah Vuono, Elizabeth Ramirez-Medina, Elizabeth Velazquez-Salinas, Lauro Zhu, James |
Author_xml | – sequence: 1 givenname: Manuel V. surname: Borca fullname: Borca, Manuel V. organization: U.S. Department of Agriculture, Agricultural Research Service, Plum Island Animal Disease Center, Greenport, New York, USA – sequence: 2 givenname: Elizabeth surname: Ramirez-Medina fullname: Ramirez-Medina, Elizabeth organization: U.S. Department of Agriculture, Agricultural Research Service, Plum Island Animal Disease Center, Greenport, New York, USA, Department of Pathobiology and Veterinary Science, University of Connecticut, Storrs, Connecticut, USA – sequence: 3 givenname: Ediane surname: Silva fullname: Silva, Ediane organization: U.S. Department of Agriculture, Agricultural Research Service, Plum Island Animal Disease Center, Greenport, New York, USA, Department of Anatomy and Physiology, Kansas State University, Manhattan, Kansas, USA – sequence: 4 givenname: Elizabeth surname: Vuono fullname: Vuono, Elizabeth organization: U.S. Department of Agriculture, Agricultural Research Service, Plum Island Animal Disease Center, Greenport, New York, USA, Department of Pathobiology and Population Medicine, Mississippi State University, Starkville, Mississippi, USA – sequence: 5 givenname: Ayushi surname: Rai fullname: Rai, Ayushi organization: U.S. Department of Agriculture, Agricultural Research Service, Plum Island Animal Disease Center, Greenport, New York, USA, Oak Ridge Institute for Science and Education (ORISE), Oak Ridge, Tennessee, USA – sequence: 6 givenname: Sarah surname: Pruitt fullname: Pruitt, Sarah organization: U.S. Department of Agriculture, Agricultural Research Service, Plum Island Animal Disease Center, Greenport, New York, USA, Oak Ridge Institute for Science and Education (ORISE), Oak Ridge, Tennessee, USA – sequence: 7 givenname: Lauren G. surname: Holinka fullname: Holinka, Lauren G. organization: U.S. Department of Agriculture, Agricultural Research Service, Plum Island Animal Disease Center, Greenport, New York, USA – sequence: 8 givenname: Lauro surname: Velazquez-Salinas fullname: Velazquez-Salinas, Lauro organization: U.S. Department of Agriculture, Agricultural Research Service, Plum Island Animal Disease Center, Greenport, New York, USA, Department of Anatomy and Physiology, Kansas State University, Manhattan, Kansas, USA – sequence: 9 givenname: James surname: Zhu fullname: Zhu, James organization: U.S. Department of Agriculture, Agricultural Research Service, Plum Island Animal Disease Center, Greenport, New York, USA – sequence: 10 givenname: Douglas P. surname: Gladue fullname: Gladue, Douglas P. organization: U.S. Department of Agriculture, Agricultural Research Service, Plum Island Animal Disease Center, Greenport, New York, USA |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/31969432$$D View this record in MEDLINE/PubMed |
BookMark | eNptkstuEzEUhi1URNOWHWvkJQum2DP2XDZIVZq2QZGQaBuxszye48TI4wm2JyiPxFvi6QUBYmNLPt__n4vPCTpygwOE3lByTmlef_i0Xp6TnNAqo80LNKOkqTPOKTtCM0LyPONF_fUYnYTwjRDKWMleoeOCNmXDinyGfl7CHuyw68FFPGgs8Y3ZbO0BL7QGFc0e8IX2RkmHb38YB_gq8R6vjR8DXkulprf2gC_BQjSDmzziFvCSVtUKX0OKfoEw2hiwSRYRvLEp2vejM_GA5UYaF-KDZD56P1Wx2JkOeqPwYvQyGJlUPlFn6KWWNsDrp_sU3V8t7uY32erz9XJ-scoU4yRm0BFOeAddak8TXjLWgWp4IVtFC9XJgnIKraQV8LbsQGqSgJpBV4NW6ShO0cdH393Y9tCpVJKXVuy86aU_iEEa8XfEma3YDHtRkZo2pEgG754M_PB9hBBFb4ICa6WDYQwiLxjL87Ju6oS-_TPX7yTP_5OA_BFQfgjBgxbKRDkNepqJFZSIaQlEWgLxsASCNkn0_h_Rs-9_8V96uLZ6 |
CitedBy_id | crossref_primary_10_3390_pathogens9121078 crossref_primary_10_3389_fimmu_2022_1093599 crossref_primary_10_1021_acsomega_0c03917 crossref_primary_10_3390_v15102064 crossref_primary_10_1128_jvi_00622_24 crossref_primary_10_3390_v13020255 crossref_primary_10_3390_v16121911 crossref_primary_10_3390_v15020566 crossref_primary_10_3390_v16081257 crossref_primary_10_3390_vaccines10121992 crossref_primary_10_3390_v15040858 crossref_primary_10_3390_v15071477 crossref_primary_10_3390_v14081731 crossref_primary_10_3390_vaccines11040762 crossref_primary_10_1016_j_biologicals_2023_101685 crossref_primary_10_1128_jvi_01977_22 crossref_primary_10_3390_v16091502 crossref_primary_10_3389_fvets_2024_1413237 crossref_primary_10_3390_v15020574 crossref_primary_10_3390_v15081722 crossref_primary_10_1128_JVI_00123_21 crossref_primary_10_4049_jimmunol_2001110 crossref_primary_10_1128_JVI_01139_21 crossref_primary_10_12968_live_2022_27_3_127 crossref_primary_10_1016_j_jbc_2023_104767 crossref_primary_10_3390_vaccines8040585 crossref_primary_10_1016_j_micpath_2021_105024 crossref_primary_10_3389_fmicb_2022_1011891 crossref_primary_10_3390_vaccines11101577 crossref_primary_10_3390_v15102089 crossref_primary_10_26416_PV_46_4_2024_10385 crossref_primary_10_1128_jvi_01106_23 crossref_primary_10_3390_v14071487 crossref_primary_10_1128_jvi_01919_21 crossref_primary_10_1016_j_vetvac_2023_100013 crossref_primary_10_1186_s12917_020_02639_2 crossref_primary_10_3390_pathogens13040319 crossref_primary_10_3390_v13091804 crossref_primary_10_3390_ani14131951 crossref_primary_10_3389_fmicb_2023_1295678 crossref_primary_10_3390_ani14172469 crossref_primary_10_3390_pathogens11090996 crossref_primary_10_3390_v13122490 crossref_primary_10_1128_JVI_01500_21 crossref_primary_10_1080_22221751_2024_2429624 crossref_primary_10_1128_jvi_00228_23 crossref_primary_10_3390_v14122619 crossref_primary_10_3389_fmicb_2022_970501 crossref_primary_10_1038_s41598_022_25987_5 crossref_primary_10_1080_22221751_2022_2148560 crossref_primary_10_3389_fmicb_2024_1469166 crossref_primary_10_1128_jvi_01030_23 crossref_primary_10_1016_j_antiviral_2022_105433 crossref_primary_10_3390_pathogens12091092 crossref_primary_10_3390_v16030376 crossref_primary_10_1073_pnas_2210808120 crossref_primary_10_1080_22221751_2023_2233643 crossref_primary_10_1128_JVI_01199_21 crossref_primary_10_1007_s11033_024_09884_w crossref_primary_10_3390_v14091912 crossref_primary_10_3389_fvets_2022_943099 crossref_primary_10_1111_tbed_13699 crossref_primary_10_1371_journal_pone_0290395 crossref_primary_10_3390_vaccines11111687 crossref_primary_10_1016_j_virs_2024_05_007 crossref_primary_10_3390_v14050896 crossref_primary_10_1016_j_vetvac_2023_100042 crossref_primary_10_2743_jve_27_99 crossref_primary_10_3390_pathogens11121438 crossref_primary_10_1080_22221751_2024_2432372 crossref_primary_10_3389_fvets_2023_1085473 crossref_primary_10_3390_v12060676 crossref_primary_10_3389_fvets_2023_1079918 crossref_primary_10_1016_j_vaccine_2024_06_020 crossref_primary_10_3390_v13081473 crossref_primary_10_1155_2024_6898157 crossref_primary_10_3390_ani13122002 crossref_primary_10_3390_v13112264 crossref_primary_10_1080_22221751_2024_2377599 crossref_primary_10_2222_jsv_70_15 crossref_primary_10_1128_JVI_01419_21 crossref_primary_10_3390_pathogens12060805 crossref_primary_10_3390_pathogens11111311 crossref_primary_10_1128_spectrum_03199_23 crossref_primary_10_1007_s00284_022_03033_x crossref_primary_10_2478_acve_2023_0002 crossref_primary_10_3389_fvets_2023_1289676 crossref_primary_10_3390_v16050731 crossref_primary_10_3390_pathogens11020145 crossref_primary_10_3389_fmicb_2023_1225469 crossref_primary_10_1007_s42770_024_01264_7 crossref_primary_10_31073_vet_biotech44_10 crossref_primary_10_3389_fimmu_2023_1186916 crossref_primary_10_3390_v13050765 crossref_primary_10_3390_vaccines9050508 crossref_primary_10_3390_v16081326 crossref_primary_10_36233_0507_4088_117 crossref_primary_10_3390_v14050878 crossref_primary_10_1186_s40813_020_00154_2 crossref_primary_10_2222_jsv_70_3 crossref_primary_10_3390_agriculture11080738 crossref_primary_10_3389_fvets_2021_768869 crossref_primary_10_4142_jvs_2021_22_e13 crossref_primary_10_3390_vaccines9030242 crossref_primary_10_1128_jvi_00247_23 crossref_primary_10_1128_jvi_00545_22 crossref_primary_10_3390_vaccines12101125 crossref_primary_10_3390_life12081255 crossref_primary_10_3390_v15081674 crossref_primary_10_1111_tbed_14191 crossref_primary_10_3390_v13071212 crossref_primary_10_3390_vaccines10030344 crossref_primary_10_3390_v15091925 crossref_primary_10_1016_j_crmicr_2024_100232 crossref_primary_10_1128_jvi_00597_22 crossref_primary_10_3390_v16091464 crossref_primary_10_3390_vaccines12101114 crossref_primary_10_3390_vaccines8040625 crossref_primary_10_1007_s00705_024_06098_0 crossref_primary_10_3389_fvets_2022_978398 crossref_primary_10_3390_ijms25010335 crossref_primary_10_3389_fimmu_2024_1397780 crossref_primary_10_1186_s13567_024_01332_8 crossref_primary_10_3390_pathogens13020103 crossref_primary_10_1016_j_vetmic_2020_108832 crossref_primary_10_3390_v13122552 crossref_primary_10_1128_mbio_00606_23 crossref_primary_10_3390_vaccines8020234 crossref_primary_10_2903_j_efsa_2021_6419 crossref_primary_10_1016_j_virusres_2023_199287 crossref_primary_10_3390_v14051112 crossref_primary_10_3390_v15112169 crossref_primary_10_1371_journal_ppat_1009733 crossref_primary_10_1360_SSV_2023_0190 crossref_primary_10_1128_jvi_00704_23 crossref_primary_10_3390_v14081682 crossref_primary_10_3389_fmicb_2021_698001 crossref_primary_10_3390_v14071409 crossref_primary_10_3390_vaccines12121443 crossref_primary_10_1186_s40249_021_00920_6 crossref_primary_10_1186_s40813_020_00179_7 crossref_primary_10_1007_s12250_021_00350_6 crossref_primary_10_3390_microorganisms13030615 crossref_primary_10_3390_v15112275 crossref_primary_10_3390_vaccines11040825 crossref_primary_10_1016_j_jbc_2021_101190 crossref_primary_10_1186_s12985_022_01747_9 crossref_primary_10_1371_journal_ppat_1010270 crossref_primary_10_3390_v12101185 crossref_primary_10_3390_v14020401 crossref_primary_10_3390_v12101193 crossref_primary_10_1038_s41541_025_01101_4 crossref_primary_10_3390_v14010053 crossref_primary_10_1038_s41598_024_80170_2 crossref_primary_10_3390_ani13233713 crossref_primary_10_1080_00480169_2021_1875934 crossref_primary_10_1007_s00253_023_12518_z crossref_primary_10_1007_s12088_022_01007_y crossref_primary_10_3390_vaccines12040407 crossref_primary_10_3390_v12090918 crossref_primary_10_1038_s41541_025_01099_9 crossref_primary_10_3390_v15040890 crossref_primary_10_3389_fmicb_2024_1345236 crossref_primary_10_3390_v13071259 crossref_primary_10_1096_fj_202201856R crossref_primary_10_1007_s11427_020_1657_9 crossref_primary_10_3390_foods9091148 crossref_primary_10_1371_journal_ppat_1010931 crossref_primary_10_1016_j_micpath_2024_107063 crossref_primary_10_3390_v16060913 crossref_primary_10_1080_22221751_2023_2300464 crossref_primary_10_3389_fimmu_2022_1002616 crossref_primary_10_3390_pathogens9121044 crossref_primary_10_3390_v13060986 crossref_primary_10_3390_v14112548 crossref_primary_10_1186_s13567_024_01386_8 crossref_primary_10_3390_v15102134 crossref_primary_10_3390_vaccines11040846 crossref_primary_10_3390_ani12141754 crossref_primary_10_1016_j_engmic_2024_100149 crossref_primary_10_1128_jvi_00231_24 crossref_primary_10_3390_v12121474 crossref_primary_10_1038_s41541_024_00845_9 crossref_primary_10_3390_v13050943 crossref_primary_10_3390_v13020286 crossref_primary_10_3389_fvets_2022_921907 crossref_primary_10_1016_j_virusres_2020_198099 crossref_primary_10_1080_22221751_2023_2265661 crossref_primary_10_3389_fmicb_2022_902932 crossref_primary_10_1016_j_virusres_2024_199343 crossref_primary_10_3390_vaccines9010029 crossref_primary_10_3390_v13010039 crossref_primary_10_3389_fmicb_2023_1139494 crossref_primary_10_3390_v13030521 crossref_primary_10_3390_v13091678 crossref_primary_10_1007_s11427_021_1904_4 crossref_primary_10_3390_v16101602 crossref_primary_10_3390_vaccines12111278 crossref_primary_10_1128_jvi_01957_21 crossref_primary_10_3389_fmicb_2022_1017792 crossref_primary_10_1016_j_virol_2024_110351 crossref_primary_10_1128_jvi_01192_22 crossref_primary_10_1128_mbio_02330_21 crossref_primary_10_1016_j_virusres_2024_199359 crossref_primary_10_3389_fvets_2022_921481 crossref_primary_10_3389_fimmu_2024_1388812 crossref_primary_10_1186_s40813_020_00159_x crossref_primary_10_3390_v14081630 crossref_primary_10_2478_jvetres_2022_0016 crossref_primary_10_3390_vaccines12121406 crossref_primary_10_1016_j_rvsc_2021_10_003 crossref_primary_10_3389_fvets_2020_00215 crossref_primary_10_1080_22221751_2024_2366406 crossref_primary_10_1128_JVI_00824_21 crossref_primary_10_1007_s00705_023_05935_y crossref_primary_10_1186_s13567_024_01407_6 crossref_primary_10_3390_v14010010 |
Cites_doi | 10.1128/JVI.00969-15 10.1016/s0065-3527(08)60714-9 10.1099/vir.0.81038-0 10.3390/v8100291 10.1128/JVI.70.12.8865-8871.1996 10.1101/847343 10.1038/s41598-018-21575-8 10.1007/bf01314703 10.1093/oxfordjournals.aje.a118408 10.1098/rstb.2009.0098 10.1128/JVI.00554-15 10.1016/j.virusres.2016.05.014 10.3390/v11090846 10.1128/JVI.72.12.10310-10315.1998 10.1006/viro.1994.1040 10.1128/JVI.01760-16 10.1007/978-3-540-68618-7_2 10.1128/JVI.72.2.1028-1035.1998 10.1016/j.virusres.2015.12.002 10.1128/jvi.74.3.1275-1285.2000 10.3201/eid1704.101283 10.3390/v11070599 10.1371/journal.pone.0223955 |
ContentType | Journal Article |
Copyright | Copyright © 2020 American Society for Microbiology. Copyright © 2020 American Society for Microbiology. 2020 American Society for Microbiology |
Copyright_xml | – notice: Copyright © 2020 American Society for Microbiology. – notice: Copyright © 2020 American Society for Microbiology. 2020 American Society for Microbiology |
DBID | AAYXX CITATION NPM 7X8 5PM |
DOI | 10.1128/JVI.02017-19 |
DatabaseName | CrossRef PubMed MEDLINE - Academic PubMed Central (Full Participant titles) |
DatabaseTitle | CrossRef PubMed MEDLINE - Academic |
DatabaseTitleList | PubMed MEDLINE - Academic CrossRef |
Database_xml | – sequence: 1 dbid: NPM name: PubMed url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed sourceTypes: Index Database |
DeliveryMethod | fulltext_linktorsrc |
Discipline | Biology |
DocumentTitleAlternate | ASFV-GΔI177L Is a Vaccine against ASFV Eurasia Strain |
EISSN | 1098-5514 |
ExternalDocumentID | PMC7081903 31969432 10_1128_JVI_02017_19 |
Genre | Journal Article |
GrantInformation_xml | – fundername: ; grantid: 70RSAT19KPM000056 – fundername: ; grantid: 70RSAT18KPM000134 |
GroupedDBID | --- -~X 0R~ 18M 29L 2WC 39C 4.4 53G 5GY 5RE 5VS 85S AAFWJ AAGFI AAYXX ABPPZ ACGFO ACNCT ADBBV AENEX AGVNZ ALMA_UNASSIGNED_HOLDINGS AOIJS BAWUL BTFSW CITATION CS3 DIK E3Z EBS F5P FRP GX1 H13 HYE HZ~ IH2 KQ8 N9A O9- OK1 P2P RHI RNS RPM RSF TR2 UPT W2D W8F WH7 WOQ YQT ~02 ~KM NPM RHF UCJ 7X8 5PM |
ID | FETCH-LOGICAL-c450t-ed0505ded432f05644dec953abc13cda3151eba17e5b6deaf04de84ed8efcd8e3 |
ISSN | 0022-538X 1098-5514 |
IngestDate | Thu Aug 21 13:56:36 EDT 2025 Fri Jul 11 12:32:41 EDT 2025 Thu Jan 02 22:58:49 EST 2025 Tue Jul 01 01:32:34 EDT 2025 Thu Apr 24 23:10:02 EDT 2025 |
IsDoiOpenAccess | false |
IsOpenAccess | true |
IsPeerReviewed | true |
IsScholarly | true |
Issue | 7 |
Keywords | African swine fever virus vaccine ASF ASFV |
Language | English |
License | Copyright © 2020 American Society for Microbiology. All Rights Reserved. |
LinkModel | OpenURL |
MergedId | FETCHMERGED-LOGICAL-c450t-ed0505ded432f05644dec953abc13cda3151eba17e5b6deaf04de84ed8efcd8e3 |
Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 Citation Borca MV, Ramirez-Medina E, Silva E, Vuono E, Rai A, Pruitt S, Holinka LG, Velazquez-Salinas L, Zhu J, Gladue DP. 2020. Development of a highly effective African swine fever virus vaccine by deletion of the I177L gene results in sterile immunity against the current epidemic Eurasia strain. J Virol 94:e02017-19. https://doi.org/10.1128/JVI.02017-19. |
OpenAccessLink | https://www.ncbi.nlm.nih.gov/pmc/articles/7081903 |
PMID | 31969432 |
PQID | 2344226898 |
PQPubID | 23479 |
ParticipantIDs | pubmedcentral_primary_oai_pubmedcentral_nih_gov_7081903 proquest_miscellaneous_2344226898 pubmed_primary_31969432 crossref_citationtrail_10_1128_JVI_02017_19 crossref_primary_10_1128_JVI_02017_19 |
ProviderPackageCode | CITATION AAYXX |
PublicationCentury | 2000 |
PublicationDate | 20200317 |
PublicationDateYYYYMMDD | 2020-03-17 |
PublicationDate_xml | – month: 3 year: 2020 text: 20200317 day: 17 |
PublicationDecade | 2020 |
PublicationPlace | United States |
PublicationPlace_xml | – name: United States – name: 1752 N St., N.W., Washington, DC |
PublicationTitle | Journal of virology |
PublicationTitleAlternate | J Virol |
PublicationYear | 2020 |
Publisher | American Society for Microbiology |
Publisher_xml | – name: American Society for Microbiology |
References | e_1_3_2_27_2 e_1_3_2_28_2 e_1_3_2_29_2 e_1_3_2_20_2 e_1_3_2_21_2 e_1_3_2_22_2 e_1_3_2_23_2 Coggins L (e_1_3_2_5_2) 1974; 18 e_1_3_2_24_2 e_1_3_2_25_2 e_1_3_2_15_2 e_1_3_2_8_2 e_1_3_2_16_2 e_1_3_2_17_2 e_1_3_2_6_2 e_1_3_2_18_2 Kihm UAM (e_1_3_2_7_2) 1987 e_1_3_2_30_2 e_1_3_2_11_2 e_1_3_2_4_2 e_1_3_2_12_2 e_1_3_2_3_2 e_1_3_2_13_2 e_1_3_2_2_2 e_1_3_2_14_2 Ruiz Gonzalvo F (e_1_3_2_19_2) 1986; 47 Hamdy FM (e_1_3_2_9_2) 1984; 45 |
References_xml | – ident: e_1_3_2_14_2 doi: 10.1128/JVI.00969-15 – ident: e_1_3_2_8_2 doi: 10.1016/s0065-3527(08)60714-9 – ident: e_1_3_2_20_2 doi: 10.1099/vir.0.81038-0 – ident: e_1_3_2_21_2 doi: 10.3390/v8100291 – ident: e_1_3_2_16_2 doi: 10.1128/JVI.70.12.8865-8871.1996 – volume: 18 start-page: 48 year: 1974 ident: e_1_3_2_5_2 article-title: African swine fever virus. Pathogenesis publication-title: Prog Med Virol – ident: e_1_3_2_30_2 doi: 10.1101/847343 – ident: e_1_3_2_29_2 doi: 10.1038/s41598-018-21575-8 – ident: e_1_3_2_6_2 doi: 10.1007/bf01314703 – ident: e_1_3_2_27_2 doi: 10.1093/oxfordjournals.aje.a118408 – ident: e_1_3_2_3_2 doi: 10.1098/rstb.2009.0098 – ident: e_1_3_2_13_2 doi: 10.1128/JVI.00554-15 – ident: e_1_3_2_15_2 doi: 10.1016/j.virusres.2016.05.014 – ident: e_1_3_2_17_2 doi: 10.3390/v11090846 – volume: 45 start-page: 711 year: 1984 ident: e_1_3_2_9_2 article-title: Clinical and immunologic responses of pigs to African swine fever virus isolated from the Western Hemisphere publication-title: Am J Vet Res – ident: e_1_3_2_12_2 doi: 10.1128/JVI.72.12.10310-10315.1998 – ident: e_1_3_2_18_2 doi: 10.1006/viro.1994.1040 – ident: e_1_3_2_23_2 doi: 10.1128/JVI.01760-16 – ident: e_1_3_2_2_2 doi: 10.1007/978-3-540-68618-7_2 – ident: e_1_3_2_22_2 doi: 10.1128/JVI.72.2.1028-1035.1998 – ident: e_1_3_2_25_2 doi: 10.1016/j.virusres.2015.12.002 – volume-title: Approaches to vaccination African swine fever year: 1987 ident: e_1_3_2_7_2 – ident: e_1_3_2_11_2 doi: 10.1128/jvi.74.3.1275-1285.2000 – ident: e_1_3_2_4_2 doi: 10.3201/eid1704.101283 – ident: e_1_3_2_24_2 doi: 10.3390/v11070599 – volume: 47 start-page: 1249 year: 1986 ident: e_1_3_2_19_2 article-title: Inhibition of African swine fever infection in the presence of immune sera in vivo and in vitro publication-title: Am J Vet Res – ident: e_1_3_2_28_2 doi: 10.1371/journal.pone.0223955 |
SSID | ssj0014464 |
Score | 2.6718836 |
Snippet | Currently, there is no commercially available vaccine against African swine fever. Outbreaks of this disease are devastating the swine industry from Central... African swine fever virus (ASFV) is the etiological agent of a contagious and often lethal disease of domestic pigs that has significant economic consequences... |
SourceID | pubmedcentral proquest pubmed crossref |
SourceType | Open Access Repository Aggregation Database Index Database Enrichment Source |
SubjectTerms | Vaccines and Antiviral Agents |
Title | Development of a Highly Effective African Swine Fever Virus Vaccine by Deletion of the I177L Gene Results in Sterile Immunity against the Current Epidemic Eurasia Strain |
URI | https://www.ncbi.nlm.nih.gov/pubmed/31969432 https://www.proquest.com/docview/2344226898 https://pubmed.ncbi.nlm.nih.gov/PMC7081903 |
Volume | 94 |
hasFullText | 1 |
inHoldings | 1 |
isFullTextHit | |
isPrint | |
link | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnZ1Zb9NAEIBXoQjUl4qblEODBE-RS2yvY_uRo1Vbjgdoo75Z6_UaIrlJlcag9Ach8S-Z2Vm7Tg8JeFlF3iNR5vPu7O4cQrz0fQr5qI3nxzr3UP-XXjoqhp4KRkUSxcGQbXM-fR7tHsr9o-io1_vVsVqqF_mWPrvSr-R_pIrPUK7kJfsPkm0HxQf4GeWLJUoYy7-Sccfih_0cyWqjWg44JDHZBHEaIHyFf5I2uYPt54PxZF6fDsZK0506qZ_vDUXgZsXRGlP6cfzRBqSm0_26Wlib2a8U1bnCWutRgrq7-qYmqFzaLk2Yp21OOKvJgYb8M-nWW7ng3pdVYPKx657qv53NtWIPomltqnMD3C_qGKfmM4-uldiJrWuOxkdEk-oH1xDxLa7jmpOLX-jgzjlwU0tGc7wWG56bKfQpKXjdyZszJDtI46vXhID8HPbHe1s4Kq7JPEV38Dg5tnzQZJRKd9q6GoO7qbohbga4HbFb970P7W0Vbqll41QRJK-7X7UubjedVzWfS9uZi1a5HTXn4I7YcMKBNwzbXdEz03viFmcsXd4XvzvIwawEBYwctMiBQw4scmCRA4scOOQgX0KDHI2B_IBFDgg5cMjBBIdg5KBBDhxytotDDhrkwCEHjNwDcbizffBu13PZPjwto-HCMwUlVSxMgX9ViWq5lIXRaRSqXPuhLlSIuqnJlR-bKB8VRpVDbJBIUySm1FiED8XadDY1jwXkOlajvEjjoZZSUS6ZtLSxDXGxKSMd9cWgkUSmXSh8-mlVZrfEQZKhCDMrwsxP--JV2_qEQ8Bc0-5FI9QM52i6eEPcZ_VpFoSSHNaTNOmLRyzkdqSGjr6IV8TfNqD476s108l3Gwc-tup8uHntmE_E-vmb9FSsLea1eYY69CJ_bgH-A0L0zTQ |
linkProvider | Flying Publisher |
openUrl | ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Development+of+a+Highly+Effective+African+Swine+Fever+Virus+Vaccine+by+Deletion+of+the+I177L+Gene+Results+in+Sterile+Immunity+against+the+Current+Epidemic+Eurasia+Strain&rft.jtitle=Journal+of+virology&rft.au=Borca%2C+Manuel+V&rft.au=Ramirez-Medina%2C+Elizabeth&rft.au=Silva%2C+Ediane&rft.au=Vuono%2C+Elizabeth&rft.date=2020-03-17&rft.eissn=1098-5514&rft.volume=94&rft.issue=7&rft_id=info:doi/10.1128%2FJVI.02017-19&rft_id=info%3Apmid%2F31969432&rft.externalDocID=31969432 |
thumbnail_l | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=0022-538X&client=summon |
thumbnail_m | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=0022-538X&client=summon |
thumbnail_s | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=0022-538X&client=summon |